Package 21130-674-52

Brand: naproxen

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 21130-674-52
Digits Only 2113067452
Product NDC 21130-674
Description

1 BOTTLE, PLASTIC in 1 CARTON (21130-674-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2023-10-04
Brand naproxen
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06f65a62-3f8d-4f00-a807-a4f4925ab16f", "openfda": {"upc": ["0321130187165"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["43745d42-f859-4168-a2dd-2c8ae47ae590"], "manufacturer_name": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (21130-674-52)  / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "21130-674-52", "marketing_start_date": "20231004"}], "brand_name": "Naproxen", "product_id": "21130-674_06f65a62-3f8d-4f00-a807-a4f4925ab16f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "21130-674", "generic_name": "Naproxen Sodium", "labeler_name": "Better Living Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20231004", "listing_expiration_date": "20261231"}